JP6841814B2 - オレフィン重合用予備重合触媒成分 - Google Patents

オレフィン重合用予備重合触媒成分 Download PDF

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Publication number: JP6841814B2
Authority: JP; Japan
Prior art keywords: catalyst component; catalyst; prepolymerization; polymerization; hydrogen
Prior art date: 2015-08-04
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Active

Application number

JP2018505462A

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English (en)

Japanese (ja)

Other versions

JP2018522128A (ja

Inventor

ジュゼッピーナ・マリア・アルゴッツィーニ

ディエゴ・ブリタ

マッシモ・センシ

ジアンニ・コリーナ

ティジアナ・ダロッコ

マリア・ディ・ディエゴ

ベネデッタ・ガッディ

オフェリア・フスコ

ジャンピエロ・モリーニ

ロレッラ・ペドリアリ

Original Assignee

バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2015-08-04

Filing date

2016-07-14

Publication date

2021-03-10

2016-07-14 Application filed by バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ filed Critical バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ

2018-08-09 Publication of JP2018522128A publication Critical patent/JP2018522128A/ja

2021-03-10 Application granted granted Critical

2021-03-10 Publication of JP6841814B2 publication Critical patent/JP6841814B2/ja

Status Active legal-status Critical Current

2036-07-14 Anticipated expiration legal-status Critical

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239000003054 catalyst Substances 0.000 title claims description 69
238000006116 polymerization reaction Methods 0.000 title claims description 47
150000001336 alkenes Chemical class 0.000 title claims description 15
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 title claims description 10
-1 polyethylene Polymers 0.000 claims description 33
239000007789 gas Substances 0.000 claims description 25
150000001875 compounds Chemical class 0.000 claims description 22
239000011949 solid catalyst Substances 0.000 claims description 19
229910052739 hydrogen Inorganic materials 0.000 claims description 18
239000001257 hydrogen Substances 0.000 claims description 18
238000000034 method Methods 0.000 claims description 16
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 12
229910052736 halogen Inorganic materials 0.000 claims description 12
150000003254 radicals Chemical class 0.000 claims description 12
230000003197 catalytic effect Effects 0.000 claims description 11
239000000460 chlorine Substances 0.000 claims description 10
150000002367 halogens Chemical class 0.000 claims description 10
229910052801 chlorine Inorganic materials 0.000 claims description 8
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 7
239000005977 Ethylene Substances 0.000 claims description 7
125000005842 heteroatom Chemical group 0.000 claims description 7
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 7
229910052749 magnesium Inorganic materials 0.000 claims description 7
239000004698 Polyethylene Substances 0.000 claims description 6
125000000753 cycloalkyl group Chemical group 0.000 claims description 6
150000002430 hydrocarbons Chemical group 0.000 claims description 6
229920000573 polyethylene Polymers 0.000 claims description 6
229910052719 titanium Inorganic materials 0.000 claims description 6
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125000004432 carbon atom Chemical group C* 0.000 claims description 5
238000006243 chemical reaction Methods 0.000 claims description 5
229910052731 fluorine Inorganic materials 0.000 claims description 5
239000011800 void material Substances 0.000 claims description 5
125000003118 aryl group Chemical group 0.000 claims description 4
229910052698 phosphorus Inorganic materials 0.000 claims description 4
229910052710 silicon Inorganic materials 0.000 claims description 4
150000003377 silicon compounds Chemical class 0.000 claims description 4
229910052717 sulfur Inorganic materials 0.000 claims description 4
125000002877 alkyl aryl group Chemical group 0.000 claims description 3
150000005840 aryl radicals Chemical class 0.000 claims description 3
125000001309 chloro group Chemical group Cl* 0.000 claims description 3
125000001183 hydrocarbyl group Chemical group 0.000 claims description 3
229910052760 oxygen Inorganic materials 0.000 claims description 3
125000001424 substituent group Chemical group 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 2
239000007795 chemical reaction product Substances 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
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239000000203 mixture Substances 0.000 description 20
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LFXVBWRMVZPLFK-UHFFFAOYSA-N trioctylalumane Chemical compound CCCCCCCC[Al](CCCCCCCC)CCCCCCCC LFXVBWRMVZPLFK-UHFFFAOYSA-N 0.000 description 5
239000012808 vapor phase Substances 0.000 description 5
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OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 4
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230000015572 biosynthetic process Effects 0.000 description 4
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
231100000640 hair analysis Toxicity 0.000 description 4
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 4
239000002861 polymer material Substances 0.000 description 4
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239000000126 substance Substances 0.000 description 4
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ZWINORFLMHROGF-UHFFFAOYSA-N 9,9-bis(methoxymethyl)fluorene Chemical compound C1=CC=C2C(COC)(COC)C3=CC=CC=C3C2=C1 ZWINORFLMHROGF-UHFFFAOYSA-N 0.000 description 3
238000013019 agitation Methods 0.000 description 3
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
SJJCABYOVIHNPZ-UHFFFAOYSA-N cyclohexyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C1CCCCC1 SJJCABYOVIHNPZ-UHFFFAOYSA-N 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
238000009826 distribution Methods 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
238000005243 fluidization Methods 0.000 description 3
238000012685 gas phase polymerization Methods 0.000 description 3
238000000265 homogenisation Methods 0.000 description 3
239000011261 inert gas Substances 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
239000000463 material Substances 0.000 description 3
238000005259 measurement Methods 0.000 description 3
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 3
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
230000003134 recirculating effect Effects 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
239000000725 suspension Substances 0.000 description 3
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
238000012360 testing method Methods 0.000 description 3
RKMGAJGJIURJSJ-UHFFFAOYSA-N 2,2,6,6-tetramethylpiperidine Chemical compound CC1(C)CCCC(C)(C)N1 RKMGAJGJIURJSJ-UHFFFAOYSA-N 0.000 description 2
AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 2
241000196324 Embryophyta Species 0.000 description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical group CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
238000002083 X-ray spectrum Methods 0.000 description 2
125000005234 alkyl aluminium group Chemical group 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
238000011109 contamination Methods 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
239000003085 diluting agent Substances 0.000 description 2
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239000010419 fine particle Substances 0.000 description 2
230000005484 gravity Effects 0.000 description 2
150000004820 halides Chemical class 0.000 description 2
150000002391 heterocyclic compounds Chemical class 0.000 description 2
150000002431 hydrogen Chemical class 0.000 description 2
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
239000004005 microsphere Substances 0.000 description 2
239000003607 modifier Substances 0.000 description 2
UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
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230000037048 polymerization activity Effects 0.000 description 2
239000001294 propane Substances 0.000 description 2
239000012265 solid product Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
150000003609 titanium compounds Chemical class 0.000 description 2
VOITXYVAKOUIBA-UHFFFAOYSA-N triethylaluminium Chemical compound CC[Al](CC)CC VOITXYVAKOUIBA-UHFFFAOYSA-N 0.000 description 2
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HPOWOWTVWZELDK-UHFFFAOYSA-N (1,3-dimethoxy-2-methylpropan-2-yl)cyclohexane Chemical compound COCC(C)(COC)C1CCCCC1 HPOWOWTVWZELDK-UHFFFAOYSA-N 0.000 description 1
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MEPSBRTXOHFWCF-UHFFFAOYSA-N (2-cyclohexyl-1,3-dimethoxypropan-2-yl)cyclohexane Chemical compound C1CCCCC1C(COC)(COC)C1CCCCC1 MEPSBRTXOHFWCF-UHFFFAOYSA-N 0.000 description 1
BEDHCUAJOBASSZ-UHFFFAOYSA-N (2-cyclopentyl-1,3-dimethoxypropan-2-yl)cyclopentane Chemical compound C1CCCC1C(COC)(COC)C1CCCC1 BEDHCUAJOBASSZ-UHFFFAOYSA-N 0.000 description 1
PJSFQEVODHCOOF-UHFFFAOYSA-N (2-ethylpiperidin-1-yl)-dimethoxy-(3,3,3-trifluoropropyl)silane Chemical compound CCC1CCCCN1[Si](CCC(F)(F)F)(OC)OC PJSFQEVODHCOOF-UHFFFAOYSA-N 0.000 description 1
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FDLMLTYTOFIPCK-UHFFFAOYSA-N 1-methoxy-2-(methoxymethyl)-3-methylpentane Chemical compound CCC(C)C(COC)COC FDLMLTYTOFIPCK-UHFFFAOYSA-N 0.000 description 1
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RTBFRGCFXZNCOE-UHFFFAOYSA-N 1-methylsulfonylpiperidin-4-one Chemical compound CS(=O)(=O)N1CCC(=O)CC1 RTBFRGCFXZNCOE-UHFFFAOYSA-N 0.000 description 1
125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 description 1
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LOGBQWSMOBPZEA-UHFFFAOYSA-N 4,4-bis(methoxymethyl)-3,5-dimethylheptane Chemical compound CCC(C)C(COC)(COC)C(C)CC LOGBQWSMOBPZEA-UHFFFAOYSA-N 0.000 description 1
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CWVKCYDPJZCDMC-UHFFFAOYSA-N 4-ethyl-1-methoxy-2-(methoxymethyl)-2-methyloctane Chemical compound CCCCC(CC)CC(C)(COC)COC CWVKCYDPJZCDMC-UHFFFAOYSA-N 0.000 description 1
VIJVFTUOJNTXCA-UHFFFAOYSA-N 4-ethyl-1-methoxy-2-(methoxymethyl)octane Chemical compound CCCCC(CC)CC(COC)COC VIJVFTUOJNTXCA-UHFFFAOYSA-N 0.000 description 1
UURZCHPNAPLYER-UHFFFAOYSA-N 4-tert-butyl-9,9-bis(methoxymethyl)fluorene Chemical compound C1=CC=C(C(C)(C)C)C2=C1C(COC)(COC)C1=CC=CC=C12 UURZCHPNAPLYER-UHFFFAOYSA-N 0.000 description 1
NDTLNHGFAUSCAE-UHFFFAOYSA-N 5,5-bis(ethoxymethyl)nonane Chemical compound CCCCC(CCCC)(COCC)COCC NDTLNHGFAUSCAE-UHFFFAOYSA-N 0.000 description 1
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UAVYNJZKEVSSFO-UHFFFAOYSA-N 5,5-bis(methoxymethyl)nonane Chemical compound CCCCC(COC)(COC)CCCC UAVYNJZKEVSSFO-UHFFFAOYSA-N 0.000 description 1
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OQYGKBOREGNKLC-UHFFFAOYSA-N 7-tert-butyl-1,1-bis(methoxymethyl)-2-methylindene Chemical compound C1=CC(C(C)(C)C)=C2C(COC)(COC)C(C)=CC2=C1 OQYGKBOREGNKLC-UHFFFAOYSA-N 0.000 description 1
XBHBMIOEDQWGPY-UHFFFAOYSA-N 7-tert-butyl-1,1-bis(methoxymethyl)indene Chemical compound C1=CC(C(C)(C)C)=C2C(COC)(COC)C=CC2=C1 XBHBMIOEDQWGPY-UHFFFAOYSA-N 0.000 description 1
UMMOCVFWWKDPNL-UHFFFAOYSA-N 9,9-bis(methoxymethyl)-1,2,3,4,5,6,7,8-octahydrofluorene Chemical compound C1CCCC2=C1C(COC)(COC)C1=C2CCCC1 UMMOCVFWWKDPNL-UHFFFAOYSA-N 0.000 description 1
MGQOPBZMDMTUQK-UHFFFAOYSA-N 9,9-bis(methoxymethyl)-1,2,3,4-tetrahydrofluorene Chemical compound C12=CC=CC=C2C(COC)(COC)C2=C1CCCC2 MGQOPBZMDMTUQK-UHFFFAOYSA-N 0.000 description 1
BJBJQWLYAGUTIO-UHFFFAOYSA-N 9,9-bis(methoxymethyl)-2,3,6,7-tetramethylfluorene Chemical compound CC1=C(C)C=C2C(COC)(COC)C3=CC(C)=C(C)C=C3C2=C1 BJBJQWLYAGUTIO-UHFFFAOYSA-N 0.000 description 1
PQRUIZPAUUOIPY-UHFFFAOYSA-N 9,9-bis(methoxymethyl)-2,7-di(propan-2-yl)fluorene Chemical compound C1=C(C(C)C)C=C2C(COC)(COC)C3=CC(C(C)C)=CC=C3C2=C1 PQRUIZPAUUOIPY-UHFFFAOYSA-N 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
238000006653 Ziegler-Natta catalysis Methods 0.000 description 1
239000011954 Ziegler–Natta catalyst Substances 0.000 description 1
VDZDYDLIDXQASZ-UHFFFAOYSA-N [1-cyclohexyl-3-methoxy-2-(methoxymethyl)propan-2-yl]cyclohexane Chemical compound C1CCCCC1C(COC)(COC)CC1CCCCC1 VDZDYDLIDXQASZ-UHFFFAOYSA-N 0.000 description 1
XMYDKOZNENQEHO-UHFFFAOYSA-N [1-methoxy-2-(methoxymethyl)-3-methylbutan-2-yl]cyclopentane Chemical compound COCC(COC)(C(C)C)C1CCCC1 XMYDKOZNENQEHO-UHFFFAOYSA-N 0.000 description 1
ZVGIBQMBZHWERX-UHFFFAOYSA-N [2-(cyclohexylmethyl)-3-methoxy-2-(methoxymethyl)propyl]cyclohexane Chemical compound C1CCCCC1CC(COC)(COC)CC1CCCCC1 ZVGIBQMBZHWERX-UHFFFAOYSA-N 0.000 description 1
URYLLQVLNOEEBA-UHFFFAOYSA-N [2-benzyl-3-methoxy-2-(methoxymethyl)propyl]benzene Chemical compound C=1C=CC=CC=1CC(COC)(COC)CC1=CC=CC=C1 URYLLQVLNOEEBA-UHFFFAOYSA-N 0.000 description 1
JSDWVMORIKLNNU-UHFFFAOYSA-N [3,3-bis(methoxymethyl)-2,4,5-triphenylcyclopenta-1,4-dien-1-yl]benzene Chemical compound COCC1(COC)C(C=2C=CC=CC=2)=C(C=2C=CC=CC=2)C(C=2C=CC=CC=2)=C1C1=CC=CC=C1 JSDWVMORIKLNNU-UHFFFAOYSA-N 0.000 description 1
RORSEGNGPOMSSV-UHFFFAOYSA-N [3,3-bis(methoxymethyl)-5-phenylpentyl]benzene Chemical compound C=1C=CC=CC=1CCC(COC)(COC)CCC1=CC=CC=C1 RORSEGNGPOMSSV-UHFFFAOYSA-N 0.000 description 1
DFBNDURJLQVNJX-UHFFFAOYSA-N [3,3-bis(methoxymethyl)inden-4-yl]-trimethylsilane Chemical compound C1=CC([Si](C)(C)C)=C2C(COC)(COC)C=CC2=C1 DFBNDURJLQVNJX-UHFFFAOYSA-N 0.000 description 1
WVEZHRZEAFZJOI-UHFFFAOYSA-N [3-methoxy-2-(methoxymethyl)-1-phenylpropyl]benzene Chemical compound C=1C=CC=CC=1C(C(COC)COC)C1=CC=CC=C1 WVEZHRZEAFZJOI-UHFFFAOYSA-N 0.000 description 1
UKEUPAFEWAEVGQ-UHFFFAOYSA-N [3-methoxy-2-(methoxymethyl)-2-methylpropyl]benzene Chemical compound COCC(C)(COC)CC1=CC=CC=C1 UKEUPAFEWAEVGQ-UHFFFAOYSA-N 0.000 description 1
JXQCBJLNEGKSCN-UHFFFAOYSA-N [4-methoxy-3-(methoxymethyl)butyl]benzene Chemical compound COCC(COC)CCC1=CC=CC=C1 JXQCBJLNEGKSCN-UHFFFAOYSA-N 0.000 description 1
AWLBWJXVYGYRNY-UHFFFAOYSA-N [4-methoxy-3-(methoxymethyl)butyl]cyclohexane Chemical compound COCC(COC)CCC1CCCCC1 AWLBWJXVYGYRNY-UHFFFAOYSA-N 0.000 description 1
IFKPQKNFYPMKNL-UHFFFAOYSA-N [5-cyclohexyl-3,3-bis(methoxymethyl)pentyl]cyclohexane Chemical compound C1CCCCC1CCC(COC)(COC)CCC1CCCCC1 IFKPQKNFYPMKNL-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
JFCQEDHGNNZCLN-UHFFFAOYSA-N anhydrous glutaric acid Natural products OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 description 1
230000001588 bifunctional effect Effects 0.000 description 1
230000000903 blocking effect Effects 0.000 description 1
150000001721 carbon Chemical group 0.000 description 1
150000001733 carboxylic acid esters Chemical class 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
238000004581 coalescence Methods 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
239000000356 contaminant Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
230000008021 deposition Effects 0.000 description 1
150000001991 dicarboxylic acids Chemical class 0.000 description 1
JWCYDYZLEAQGJJ-UHFFFAOYSA-N dicyclopentyl(dimethoxy)silane Chemical compound C1CCCC1[Si](OC)(OC)C1CCCC1 JWCYDYZLEAQGJJ-UHFFFAOYSA-N 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
AHUXYBVKTIBBJW-UHFFFAOYSA-N dimethoxy(diphenyl)silane Chemical compound C=1C=CC=CC=1[Si](OC)(OC)C1=CC=CC=C1 AHUXYBVKTIBBJW-UHFFFAOYSA-N 0.000 description 1
DIJRHOZMLZRNLM-UHFFFAOYSA-N dimethoxy-methyl-(3,3,3-trifluoropropyl)silane Chemical compound CO[Si](C)(OC)CCC(F)(F)F DIJRHOZMLZRNLM-UHFFFAOYSA-N 0.000 description 1
125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
238000011038 discontinuous diafiltration by volume reduction Methods 0.000 description 1
238000001035 drying Methods 0.000 description 1
230000009977 dual effect Effects 0.000 description 1
239000012634 fragment Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000008240 homogeneous mixture Substances 0.000 description 1
230000001788 irregular Effects 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000007791 liquid phase Substances 0.000 description 1
238000012423 maintenance Methods 0.000 description 1
238000010907 mechanical stirring Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
229940078552 o-xylene Drugs 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
239000002685 polymerization catalyst Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
NETBVGNWMHLXRP-UHFFFAOYSA-N tert-butyl-dimethoxy-methylsilane Chemical compound CO[Si](C)(OC)C(C)(C)C NETBVGNWMHLXRP-UHFFFAOYSA-N 0.000 description 1
238000012546 transfer Methods 0.000 description 1
SQBBHCOIQXKPHL-UHFFFAOYSA-N tributylalumane Chemical compound CCCC[Al](CCCC)CCCC SQBBHCOIQXKPHL-UHFFFAOYSA-N 0.000 description 1
MCULRUJILOGHCJ-UHFFFAOYSA-N triisobutylaluminium Chemical compound CC(C)C[Al](CC(C)C)CC(C)C MCULRUJILOGHCJ-UHFFFAOYSA-N 0.000 description 1
239000003039 volatile agent Substances 0.000 description 1

Classifications

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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F110/04—Monomers containing three or four carbon atoms
- C08F110/06—Propene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F10/04—Monomers containing three or four carbon atoms
- C08F10/06—Propene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/01—Processes of polymerisation characterised by special features of the polymerisation apparatus used
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/642—Component covered by group C08F4/64 with an organo-aluminium compound
- C08F4/6421—Titanium tetrahalides with organo-aluminium compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
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- C08F4/646—Catalysts comprising at least two different metals, in metallic form or as compounds thereof, in addition to the component covered by group C08F4/64
- C08F4/6465—Catalysts comprising at least two different metals, in metallic form or as compounds thereof, in addition to the component covered by group C08F4/64 containing silicium
- C—CHEMISTRY; METALLURGY
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- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
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- C08F4/6491—Catalysts containing a specific non-metal or metal-free compound organic hydrocarbon
- C08F4/6492—Catalysts containing a specific non-metal or metal-free compound organic hydrocarbon containing aliphatic unsaturation
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
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- C08F4/649—Catalysts containing a specific non-metal or metal-free compound organic
- C08F4/6494—Catalysts containing a specific non-metal or metal-free compound organic containing oxygen
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
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- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
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- C08F4/651—Pretreating with non-metals or metal-free compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/42—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors
- C08F4/44—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides
- C08F4/60—Metals; Metal hydrides; Metallo-organic compounds; Use thereof as catalyst precursors selected from light metals, zinc, cadmium, mercury, copper, silver, gold, boron, gallium, indium, thallium, rare earths or actinides together with refractory metals, iron group metals, platinum group metals, manganese, rhenium technetium or compounds thereof
- C08F4/62—Refractory metals or compounds thereof
- C08F4/64—Titanium, zirconium, hafnium or compounds thereof
- C08F4/65—Pretreating the metal or compound covered by group C08F4/64 before the final contacting with the metal or compound covered by group C08F4/44
- C08F4/652—Pretreating with metals or metal-containing compounds
- C08F4/654—Pretreating with metals or metal-containing compounds with magnesium or compounds thereof
- C08F4/6543—Pretreating with metals or metal-containing compounds with magnesium or compounds thereof halides of magnesium
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/34—Polymerisation in gaseous state
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2410/00—Features related to the catalyst preparation, the catalyst use or to the deactivation of the catalyst
- C08F2410/06—Catalyst characterized by its size
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/12—Melt flow index or melt flow ratio
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/15—Isotactic
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2500/00—Characteristics or properties of obtained polyolefins; Use thereof
- C08F2500/18—Bulk density

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Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Emergency Medicine (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Polymerisation Methods In General (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)

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Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BR112018002018B1 (pt) *	2015-08-04	2022-05-17	Basell Poliolefine Italia S.R.L.	Componente catalisador pré-polimerizado, sistema de catalisador e processo em fase gasosa para polimerização de olefinas
US11401356B2 (en) *	2017-07-19	2022-08-02	China Petroleum & Chemical Corporation	Olefin polymerization catalyst comprising cyclotriveratrylene and derivatives thereof
US11866522B2 (en)	2018-12-28	2024-01-09	Braskem S.A.	Process for introducing catalyst in a polymerization process
US20240209125A1 (en)	2021-04-16	2024-06-27	Basell Poliolefine Italia S.R.L.	Prepolymerized catalyst components for the polymerization of olefins
CA3231623A1 (en)	2021-09-20	2023-03-23	Dow Global Technologies Llc	Process of making catalytically-active prepolymer composition and compositions made thereby

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SE363977B (ru)	1968-11-21	1974-02-11	Montedison Spa
YU35844B (en)	1968-11-25	1981-08-31	Montedison Spa	Process for obtaining catalysts for the polymerization of olefines
IT1098272B (it)	1978-08-22	1985-09-07	Montedison Spa	Componenti,di catalizzatori e catalizzatori per la polimerizzazione delle alfa-olefine
CA1235543A (en)	1984-09-12	1988-04-19	Norio Kashiwa	Process for producing propylene block copolymer
DE3730022A1 (de)	1987-09-08	1989-03-16	Basf Ag	Verfahren zum herstellen von homo- und copolymerisaten des propens mittels eines ziegler-natta-katalysatorsystems
FR2646426B2 (fr)	1988-09-13	1991-08-16	Bp Chemicals Sa	Procede et appareillage de polymerisation d'alpha-olefine en phase gazeuse en presence d'un agent ralentisseur d'activite
CA2289027A1 (en) *	1998-03-23	1999-09-30	Montell Technology Company B.V.	Prepolymerized catalyst components for the polymerization of olefins
HUP0004633A3 (en)	1998-07-08	2003-07-28	Montell Technology Company Bv	Process and apparatus for the gas-phase polymerisation
IT1301990B1 (it) *	1998-08-03	2000-07-20	Licio Zambon	Catalizzatori per la polimerizzazione delle olefine.
ITMI991552A1 (it) *	1999-07-14	2001-01-14	Licio Zambon	Componenti di catalizzatori per la polimerizzazione di olefine
BR0205691A (pt) *	2001-06-26	2003-07-15	Basell Poliolefine Spa	Componentes e catalisadores para a polimerização de olefinas
EP1668046B8 (en)	2003-09-23	2021-04-21	W.R. Grace & CO. - CONN.	Self limiting catalyst composition and propylene polymerization process
US7942572B2 (en) *	2003-10-16	2011-05-17	Basell Poliolefine Italia S.R.L.	Process for the continuous production of emulsions
JP2010514905A (ja)	2006-12-29	2010-05-06	フイナ・テクノロジー・インコーポレーテツド	ポリプロピレンフィルムグレード樹脂製造用ｎ−ブチルメチルジメトキシシラン使用スクシネート含有重合触媒系
KR101021758B1 (ko) *	2007-10-02	2011-03-15	주식회사 엘지화학	전중합 단계를 포함하는 고투명성 폴리프로필렌의 제조방법
EP2070954A1 (en)	2007-12-14	2009-06-17	Total Petrochemicals Research Feluy	Process for the production of a propylene polymer having a broad molecular weight distribution and a low ash content
JP2011508037A (ja) *	2007-12-28	2011-03-10	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	オレフィン類の重合用触媒成分
KR101769275B1 (ko)	2009-06-19	2017-08-18	바셀 폴리올레핀 이탈리아 에스.알.엘	내충격성 프로필렌 중합체 조성물의 제조 방법
SG181835A1 (en)	2009-12-21	2012-08-30	Dow Global Technologies Llc	Gas-phase polymerization process having multiple flow regimes
JP5695869B2 (ja) *	2010-09-28	2015-04-08	日本ポリエチレン株式会社	チーグラー・ナッタ触媒の改質方法および改質されたチーグラー・ナッタ触媒、並びにそれを用いたオレフィンの重合方法および得られたオレフィン系重合体
JP6005726B2 (ja) *	2011-04-12	2016-10-12	バーゼル・ポリオレフィン・イタリア・ソチエタ・ア・レスポンサビリタ・リミタータ	オレフィン重合用の触媒成分
EP2594593A1 (en) *	2011-11-17	2013-05-22	Basell Poliolefine Italia S.r.l.	Process for the preparation of heterophasic propylene polymer compositions
EP2607386A1 (en) *	2011-12-23	2013-06-26	Basell Poliolefine Italia S.r.l.	Pre-polymerized catalyst components for the polymerization of olefins
CN103788259B (zh)	2012-10-30	2017-05-31	中国石油化工股份有限公司	一种分子量窄分布聚丙烯
KR101768846B1 (ko) *	2013-03-15	2017-08-17	바셀 폴리올레핀 이탈리아 에스.알.엘	프로필렌 삼원중합체의 제조 공정, 및 그에 의해 얻은 프로필렌 삼원중합체
EP3060588B1 (en) *	2013-10-24	2018-03-21	Basell Poliolefine Italia S.r.l.	Process for the preparation of porous propylene polymers
WO2015062787A1 (en) *	2013-10-30	2015-05-07	Basell Poliolefine Italia S.R.L.	Multimodal copolymers of propylene and 1-hexene
BR112018002018B1 (pt) *	2015-08-04	2022-05-17	Basell Poliolefine Italia S.R.L.	Componente catalisador pré-polimerizado, sistema de catalisador e processo em fase gasosa para polimerização de olefinas

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CA2994495A1 (en)	2017-02-09
EP3331926A1 (en)	2018-06-13
BR112018002018A2 (pt)	2018-09-18
RU2721530C2 (ru)	2020-05-19
JP7102075B2 (ja)	2022-07-19
RU2018104667A3 (ru)	2019-12-13
KR20190116578A (ko)	2019-10-14
WO2017021454A1 (en)	2017-02-09
BR112018001846A2 (pt)	2018-09-18
WO2017021122A1 (en)	2017-02-09
JP2018526494A (ja)	2018-09-13
EP3331927A1 (en)	2018-06-13
CN107873037A (zh)	2018-04-03
KR20180028486A (ko)	2018-03-16
KR20180030086A (ko)	2018-03-21
FI3331926T3 (fi)	2023-06-21
CA2994495C (en)	2020-09-01
US10730974B2 (en)	2020-08-04
US20180230253A1 (en)	2018-08-16
RU2018104680A3 (ru)	2019-10-02
BR112018002018B1 (pt)	2022-05-17
CN107873036B (zh)	2021-03-30
CN107873036A (zh)	2018-04-03
US10435490B2 (en)	2019-10-08
RU2717314C2 (ru)	2020-03-20
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EP3331926B1 (en)	2023-05-31
KR102056017B1 (ko)	2020-01-14
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Publication	Publication Date	Title
JP6005726B2 (ja)	2016-10-12	オレフィン重合用の触媒成分
JP6841814B2 (ja)	2021-03-10	オレフィン重合用予備重合触媒成分
EP2225287B1 (en)	2011-08-31	Catalyst components for the polymerization of olefins
US11034781B2 (en)	2021-06-15	Catalyst components for the polymerization of olefins and catalysts therefrom obtained
JP5140764B2 (ja)	2013-02-13	オレフィン重合用の触媒成分
JP2011506718A (ja)	2011-03-03	改良された特性を有する高立体規則性ポリプロピレン
CN108117617B (zh)	2021-05-04	一种用于烯烃聚合的固体催化剂组分和催化剂
US20240209125A1 (en)	2024-06-27	Prepolymerized catalyst components for the polymerization of olefins
ES2372351T3 (es)	2012-01-19	Componentes de catalizadores para la polimerización de olefinas.